Development of combined-supramolecular microextraction with ultra-performance liquid chromatography-tandem mass spectrometry procedures for ultra-trace analysis of carbaryl in water, fruits and vegetables

ALOthman Z. A., YILMAZ E., Habila M. A., Alhenaki B., SOYLAK M., Ahmed A. Y. B. H., ...Daha Fazla

International Journal of Environmental Analytical Chemistry, cilt.102, sa.7, ss.1491-1501, 2022 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 102 Sayı: 7
  • Basım Tarihi: 2022
  • Doi Numarası: 10.1080/03067319.2020.1738419
  • Dergi Adı: International Journal of Environmental Analytical Chemistry
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Aquatic Science & Fisheries Abstracts (ASFA), CAB Abstracts, Chemical Abstracts Core, Chimica, Compendex, Environment Index, Food Science & Technology Abstracts, Pollution Abstracts, Veterinary Science Database
  • Sayfa Sayıları: ss.1491-1501
  • Anahtar Kelimeler: Supramolecular solvent microextraction, carbaryl, ultra-performance liquid chromatography-tandem mass spectrometry, preconcentration, separation, CLOUD-POINT EXTRACTION, SOLID-PHASE EXTRACTION, ATOMIC-ABSORPTION-SPECTROMETRY, AL-QASSIM REGION, SOLVENT MICROEXTRACTION, ENVIRONMENTAL-SAMPLES, HEAVY-METALS, LEAD II, PESTICIDES, COPPER
  • Kayseri Üniversitesi Adresli: Hayır

Özet

© 2020 Informa UK Limited, trading as Taylor & Francis Group.For the fast and selective preconcentration-separation of carbaryl from environmental samples, a simple and cheap supramolecular solvent microextraction method (Ss-ME) has been applied with ultra-performance liquid chromatography-tandem mass spectrometry. Various analytical parameters that have a noticeable effect on the extraction of carbaryl by supramolecular liquid phase microextraction were optimised by selecting the peak area as the response. The parameters including pH of solution, type and volume of supramolecular formula, matrix effect and the sample volume were optimised. The quantitative recoveries were obtained between pH 2.0 and 4.0 of sample solution phase by using a supramolecular phase consist of heptanol and tetrahydrofuran. The limit of detection and limit of quantification were 0.03 mg L−1 and 0.09 mg L−1 respectively. The relative standard deviation was 7.11 and the preconcentration factor was 15. The microextraction procedure for trace carbaryl was used for various samples such as fruits, vegetables and water samples with the recovery% range between 90% and 102%.